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Submitted: 24 September 2012 Modified: 29 May 2013

Herdin Record #: NCR-RITM-12092410000973

Rapid identification of dengue virus serotypes by using polymerase chain reaction


1Kouichi Morita Author
2Mariko Tanaka Author
3Akira Igarashi Author

Related Institutions

Institutions NameRole
Department of Virology - Institute of tropical Medicine Nagasaki University Authors Affiliation

Publication Information

Publication Type:
Publication Sub Type:
Journal Article, Original
Journal of Clinical Microbiology
Publication Date:
October 1991
American Society for Microbiology


Four primer pairs were selected on the basis of the published sequence data of four dengue virus serotypes so that each unique target sequence size could be amplified for each serotype by polymerase chain reaction. The procedure consists of (i) RNA preparation, (ii) reverse transcription, and (iii) polymerase chain reaction, all of which could be completed within 2 h in a single tube for each specimen. The amplified sequence size revealed by ethidium bromide-stained agarose gel electrophoresis was unique for each serotype, using infected culture fluid of isolates from dengue fever or dengue hemorrhagic fever patients in Thailand, Indonesia, and the Philippines as well as from prototype viruses, thus facilitating simultaneous identification and typing.

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